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药物残留溶剂的监控及其分析方法
引用本文:胡昌勤,刘颖. 药物残留溶剂的监控及其分析方法[J]. 药学学报, 2007, 42(12): 1237-1242
作者姓名:胡昌勤  刘颖
作者单位:中国药品生物制品检定所,北京,100050
摘    要:
当药品中所含的残留溶剂水平高于安全值时,对人体或环境将产生危害。对残留溶剂的控制已越来越受到人们的关注。本文详细介绍了各国药典对残留溶剂控制标准的沿革、残留溶剂分析方法的沿革,并对近年来残留溶剂分析方法的新进展进行了综述。最后,作者根据本课题组的相关研究成果,对残留溶剂测定专家系统的应用前景进行了展望。

关 键 词:药品  残留溶剂  监控
文章编号:0513-4870(2007)12-1237-06
收稿时间:2007-06-11
修稿时间:2007-06-11

Regulations of residual solvents in pharmaceuticals and advances in the research of its analytical methods
HU Chang-qin,LIU Ying. Regulations of residual solvents in pharmaceuticals and advances in the research of its analytical methods[J]. Acta pharmaceutica Sinica, 2007, 42(12): 1237-1242
Authors:HU Chang-qin  LIU Ying
Affiliation:National Institute for the Control of Pharmaceutical and Biological Products, Beijing 100050, China. hucq@nicpbp.org.cn
Abstract:
If the presence of residual solvents in pharmaceuticals exceeds tolerance limits as suggested by safety data,they may be harmful to the human body or the environment.It is because of this that the determination of residual solvents receives a great deal of attention.This paper reviews in detail the changes in the regulations on residual solvents in pharmaceuticals in leading pharmacopoeias,and the advances in the techniques involved,especially,the recent advances in the analytical techniques are summarized.At the end,the authors introduce the prospect of the expert system for determining residual solvents in pharmaceuticals based on the studies of their research group.
Keywords:pharmaceutical  residual solvent  regulation
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